A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482918



Internal ID21140471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43557288..43557723hg38UCSC Ensembl
chr13:44131424..44131859hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009081
Samples
Known GenesENOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer